Congenital enteropathy due to enteropeptidase deficiency

A rare, genetic, gastroenterological disease characterized by early-onset failure to thrive, edema, hypoproteinemia, diarrhea and fat malabsorption (or steatorrhea) in the presence of very low or absent trypsin activity in duodenal fluid. Celiac disease, or other pancreatic or mucosal disorders, may be associated.

Also known as: congenital enterokinase deficiency, enterokinase deficiency, enteropeptidase deficiency

0 clinical trials for this condition and its sub-types, 0 tagged with Congenital enteropathy due to enteropeptidase deficiency itself.